Katiuska Tuttis, Daryne Lu Maldonado Gomes da Costa, Higor Lopes Nunes, Ana Flávia Leal Specian, Juliana Mara Serpeloni, Lourdes Campaner Dos Santos, Eliana Aparecida Varanda, Wagner Vilegas, Wilner Martínez-Lopez, Ilce Mara de Syllos Cólus
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The hydroalcoholic extract from P. ramiflora leaves consisted of flavonoids identified and quantified as myricetin-3-O-β-D-galactopyranoside (13.55 mg/g) and myricetin-3-O-α-L-rhamnopyranoside (9.61 mg/g). The extract exhibited cytotoxicity at concentrations higher than 1.5 µg/ml in human hepatocarcinoma (HepG2)and 2.5 µg/ml in non-tumoral primary gastric (GAS) cells using the MTT assay, and at concentrations higher than 3 µg/ml in HepG2 and 3.5 µg/ml in GAS cells by the neutral red assay. The extract did not show antiproliferative effect as evidenced by the nuclear division index (NDI). However, in the presence of benzo[a]pyrene (BaP) (positive control), an enhanced cytostatic effect in the NDI and flow cytometry was noted. It is of interest that when the extract was co-incubated with BaP a significant decrease in DNA damage was observed indicating an antimutagenic action. This protective effect might be attributed to myricetin and gallic acid found in P. ramiflora extract. The low cytotoxicity action and protective effect observed in the present study encourage further studies regarding other biological effects of P. ramiflora, as well as its potential use as a chemopreventive agent.</p>","PeriodicalId":17418,"journal":{"name":"Journal of Toxicology and Environmental Health, Part A","volume":" ","pages":"792-804"},"PeriodicalIF":0.0000,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/15287394.2018.1491911","citationCount":"21","resultStr":"{\"title\":\"Pouteria ramiflora (Mart.) 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引用次数: 21
摘要
紫叶菜豆(Mart.)Radlk。在巴西,它通常被用作治疗蠕虫感染、痢疾、疼痛、炎症、高脂血症和肥胖的药用植物。目前,这种提取物用于人体治疗的安全性仍有待确定。因此,本研究的目的是研究该提取物的细胞毒性、抗增殖和抗诱变作用。水杨花叶水醇提取物中黄酮类化合物为杨梅素-3- o -β- d -半乳糖吡喃苷(13.55 mg/g)和杨梅素-3- o -α- l -鼠李糖吡喃苷(9.61 mg/g)。MTT实验显示,在人肝癌(HepG2)和非肿瘤原发性胃(GAS)细胞中,浓度高于1.5µg/ml和2.5µg/ml的提取物具有细胞毒性;在中性红实验中,浓度高于3µg/ml和3.5µg/ml的提取物在胃癌细胞中具有细胞毒性。核分裂指数(NDI)表明,提取物不具有抗增殖作用。然而,在苯并[a]芘(BaP)(阳性对照)的存在下,在NDI和流式细胞术中发现了增强的细胞抑制作用。有趣的是,当提取物与BaP共孵育时,观察到DNA损伤显著减少,表明具有抗诱变作用。这种保护作用可能是由杨梅素和没食子酸所引起的。本研究中观察到的低细胞毒性作用和保护作用鼓励进一步研究分枝杆菌的其他生物学效应,以及它作为化学预防剂的潜在用途。
Pouteria ramiflora (Mart.) Radlk. extract: Flavonoids quantification and chemopreventive effect on HepG2 cells.
Pouteria ramiflora (Mart.) Radlk., popularly known as curriola, is commonly used in Brazil as medicinal plant to treat worm infections, dysentery, pain, inflammation, hyperlipidemia, and obesity. At present the safety of this extract when used therapeutically in human remains to be determined. Thus, the aim of this study was to examine cytotoxicity, antiproliferative, and antimutagenic actions of this extract. The hydroalcoholic extract from P. ramiflora leaves consisted of flavonoids identified and quantified as myricetin-3-O-β-D-galactopyranoside (13.55 mg/g) and myricetin-3-O-α-L-rhamnopyranoside (9.61 mg/g). The extract exhibited cytotoxicity at concentrations higher than 1.5 µg/ml in human hepatocarcinoma (HepG2)and 2.5 µg/ml in non-tumoral primary gastric (GAS) cells using the MTT assay, and at concentrations higher than 3 µg/ml in HepG2 and 3.5 µg/ml in GAS cells by the neutral red assay. The extract did not show antiproliferative effect as evidenced by the nuclear division index (NDI). However, in the presence of benzo[a]pyrene (BaP) (positive control), an enhanced cytostatic effect in the NDI and flow cytometry was noted. It is of interest that when the extract was co-incubated with BaP a significant decrease in DNA damage was observed indicating an antimutagenic action. This protective effect might be attributed to myricetin and gallic acid found in P. ramiflora extract. The low cytotoxicity action and protective effect observed in the present study encourage further studies regarding other biological effects of P. ramiflora, as well as its potential use as a chemopreventive agent.